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Liquidia Corporation reported initial commercial sales following FDA approval of YUTREPIA and posted early-stage revenue while remaining loss-making. YUTREPIA was approved by the FDA on May 23, 2025 and commercially launched on June 2, 2025; product sales for the three months ended June 30, 2025 were $6.5 million and service revenue (from the Sandoz promotion agreement) was $2.3 million, producing total revenue of $8.8 million for the quarter and $12.0 million for the six months.
The company reported a net loss of $41.6 million for the quarter and $79.9 million for the six months, driving an accumulated deficit of $637.3 million. Cash and cash equivalents were $173.4 million and total assets were $257.4 million. Total liabilities rose to $242.2 million driven by long-term debt (carrying value $193.6 million) and litigation finance obligations. Stockholders' equity declined to $15.2 million. The company disclosed ongoing patent and related litigation with United Therapeutics that could affect YUTREPIA, an indemnification asset of $8.3 million and a litigation finance payable of $8.0 million. Management states available cash and anticipated YUTREPIA inflows are expected to satisfy obligations for at least the next twelve months, and the HCR revenue interest financing contains a $15.0 million minimum cash covenant.
Liquidia Corporation furnished a press release announcing its financial results for the quarter ended June 30, 2025 and provided a corporate update. The press release is attached to the Form 8-K as Exhibit 99.1, and the filing includes an Inline XBRL cover page file as Exhibit 104.
The disclosure in Item 2.02 is furnished rather than filed and therefore is not deemed filed under Section 18 of the Exchange Act. No financial figures, operational details or transaction terms are included in this 8-K itself; the substantive results and update are contained in the referenced press release.